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The relationship between the structural characteristics of α-Fe2O3 catalysts and their lattice oxygen reactivity regarding hydrogen / N. Kirik, A. Krylov, A. Boronin [et al.] // Materials. - 2023. - Vol. 16, Is. 12 : The 15th Anniversary of Materials — Recent Advances in Catalytic Materials. - Ст. 4466, DOI 10.3390/ma16124466. - Cited References: 63. - This work was conducted within the framework of the budget project for the Institute of Chemistry and Chemical Technology of the Siberian Branch of the Russian Academy of Sciences, Federal Research Center KSC SB RAS, No. FWES–2021–0013 . - ISSN 1996-1944
Кл.слова (ненормированные):
α-Fe2O3 -- catalysts -- calcinations -- XRD -- XPS -- Raman spectroscopy characterization -- temperature-programmed reduction
Аннотация: In this paper, the relationship between the structural features of hematite samples calcined in the interval of 800–1100 °C and their reactivity regarding hydrogen studied in the temperature-programmed reaction (TPR-H2) was studied. The oxygen reactivity of the samples decreases with the increasing calcination temperature. The study of calcined hematite samples used X-ray Diffraction (XRD), Scanning Electron Microscopy (SEM), X-ray Photoelectron Spectroscopy (XPS), and Raman spectroscopy, and their textural characteristics were studied also. According to XRD results, hematite samples calcined in the temperature range under study are monophase, represented by the α-Fe2O3 phase, in which crystal density increases with increasing calcination temperature. The Raman spectroscopy results also register only the α-Fe2O3 phase; the samples consist of large, well-crystallized particles with smaller particles on their surface, having a significantly lower degree of crystallinity, and their proportion decreases with increasing calcination temperature. XPS results show the α-Fe2O3 surface enriched with Fe2+ ions, whose proportion increases with increasing calcination temperature, which leads to an increase in the lattice oxygen binding energy and a decrease in the α-Fe2O3 reactivity regarding hydrogen.

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Держатели документа:
Federal Research Center “Krasnoyarsk Science Center of Siberian Branch of the Russian Academy of Sciences”, Institute of Chemistry and Chemical Technology, 50/24, Akademgorodok, 660036 Krasnoyarsk, Russia
Federal Research Center “Krasnoyarsk Science Center of Siberian Branch of the Russian Academy of Sciences”, Kirensky Institute of Physics, 50/38, Akademgorodok, 660036 Krasnoyarsk, Russia
Federal Research Center Boreskov Institute of Catalysis, 5, Ac. Lavrentieva Ave., 630090 Novosibirsk, Russia
Department of Chemistry, 79, Svobodny Ave., Siberian Federal University, 660041 Krasnoyarsk, Russia

Доп.точки доступа:
Kirik, N.; Krylov, A. S.; Крылов, Александр Сергеевич; Boronin, A.; Koshcheev, S.; Solovyov, L.; Rabchevskii, E.; Shishkina, N.; Anshits, A.
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    Применение процессного моделирования для интерпретации вариации стабильных изотопов в годичных кольцах деревьев / Н. Д. Васильева, С. Н. Софронова, В. В. Баринов [и др.] // Лесотехнич. журн. - 2023. - Т. 13, № 4, Ч. 2. - С. 23-38 ; Forest. Eng. J., DOI 10.34220/issn.2222-7962/2023.4/15. - Библиогр.: 33. - Исследование выполнено за счет гранта Российского научного фонда № 21-17-00006, (https://rscf.ru/en/project/21-17-00006/) . - ISSN 2222-7962
   Перевод заглавия: Application of process-based modelling for interpretation of stable isotope variations in tree rings
Кл.слова (ненормированные):
дендрохрогология -- стабильные изотопы -- моделирование -- углерод -- кислород -- водород -- dendrochronology -- stable isotopes -- modelling -- carbon -- oxygen -- hydrogen
Аннотация: Ширина годичных колец деревьев и изотопный состав стабильных изотопов углерода (δ13C), кислорода (δ18O) и водорода (δ2H) в целлюлозе годичных колец широко используются для реконструкций условий окружающей среды. Применение моделей, способных описать вариацию стабильных изотопов в годичных кольцах деревьев, представляет собой набор инструментов для интерпретации изменений окружающей среды на экофизиологическом уровне. В данной работе хронологии с погодичным временным разрешением, полученные по стабильным изотопам δ13С, δ18O и δ2H в целлюлозе годичных колец хвойных для региона Дельта реки Маккензи в Канаде (68° 30′ с.ш., 133° 48′ з.д.) для периода с 1901 по 2009 гг., были сопоставлены с модельными расчетами для интерпретации экофизиологического сигнала. При помощи процессной модели (LPX) нам удалось смоделировать δ13С вариацию, значимо коррелирующую с измеренными данными (r = 0.29; p = 0.002) для периода с 1901 по 2009 гг. Модельные расчеты по кислороду и водороду требуют дальнейшего преобразования модельных блоков, в частности, требуют доработки включения источника воды, используемой деревьями, блока оттаивания и промерзания почвы с учетом вечной мерзлоты, а также экспериментальных данных по содержанию δ18O и δ2H в воде.
Tree-ring width and stable isotopes (carbon, oxygen, and hydrogen) in tree-ring cellulose are widely used to reconstruct environmental conditions. The application of models capable to describe a variation of stable isotopes in annual tree rings can be a powerful tool for interpretation of environmental changes at the eco-physiological level. In this paper, we modelled carbon (δ13С), oxygen (δ18O), and hydrogen (δ2H) variations at the tree-ring level and compared results with measured data, obtained from the Mackenzie Delta River (68°30′ N, 133°48′ W) for the common period from 1901 to 2009. Using a process-based model (LPX), we were able to simulate carbon isotope values, which significantly (r = 0.29; p = 0.002) correlate with measured carbon isotope values. The model calculations for oxygen and hydrogen require further modifications and improvements, in particular the inclusion of the source of water used by the trees in the Canadian subarctic, as well as δ18O and δ2H in the water.

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Сибирский Федеральный Университет, 660041, пр. Свободный, 79, Красноярск, Российская Федерация
Институт физики им. Л.В. Киренского СО РАН, Академгородок, 50, г. Красноярск, Российская Федерация, 660036
Сибирский государственный университет науки и технологий имени академика М.Ф. Решетнева, Красноярск, Красноярский рабочий 31, 660037, Российская Федерация

Доп.точки доступа:
Васильева, Наталья Дмитриевна; Vasilieva, N. D.; Софронова, Светлана Николаевна; Sofronova, S. N.; Баринов, В. В.; Тайник, А. В.; Трушкина, Т. В.; Чуракова, О. В.; РусДендро-2023, Международная дендрохронологическая конференция(5 ; сентябрь 2023г. ; Воронеж)

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Strong hydrogen bond in the crystal structure design of CuNbOF5·4H2O / N. M. Laptash, A. A. Udovenko, A. D. Vasiliev, E. B. Merkulov // J. Solid State Chem. - 2023. - Vol. 318. - Ст. 123781, DOI 10.1016/j.jssc.2022.123781. - Cited References: 40. - We thank Dr. T.B. Emelina for the DFT calculations of uncoordinated [NbOF5]2– anion. The work was partially supported within the frames of the State Order of the Institute of Chemistry, Far Eastern Branch of the Russian Academy of Sciences (project No. FWFN 0205–2022–0003) . - ISSN 0022-4596. - ISSN 1095-726X
Кл.слова (ненормированные):
Mixed transition metal oxyfluoride -- Crystal structure -- Strong hydrogen bond -- Phase transition -- Thermal analysis
Аннотация: Fluoride metal-organic frameworks (MOFs) based on pillared [NbOF5]2– anion have been recently received research attention as ultramicroporous materials for gas storage and separation. The trans-directing property of the NbOF5 octahedron plays a significant role in designing mixed metal oxyfluoride compounds composed of the alternating transition metal polyhedra, which are linked via oxide and fluoride ligands. Mixed metal CuNbOF5·4H2O is the only unique example when the trans-directing properties of [NbOF5]2– are realized in the formation of a strong O–H⋯F hydrogen bond (HB). Well-shaped single crystals of this compound were grown and their structure was refined by X-ray diffraction. Under quasi-isobaric conditions, a phase transition at 88 °C takes place, which is associated with the weakening of HBs and formation of ordinary chains through conventional trans-(O,F) bridges. The character of hydrogen bonding in CuNbOF5·4H2O affects its thermal behavior described by the dehydration and pyrohydrolysis processes.

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Держатели документа:
Institute of Chemistry, Far Eastern Branch of RAS, 159 Pr. Stoletiya Vladivostoka, Vladivostok, 690022, Russian Federation
Kirensky Institute of Physics, Siberian Branch of RAS, Academgorodok, Krasnoyarsk, 660036, Russian Federation

Доп.точки доступа:
Laptash, N. M.; Udovenko, A. A.; Vasiliev, A. D.; Васильев, Александр Дмитриевич; Merkulov, E. B.
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Novel Janus 2D structures of XMoY (X, Y = O, S, Se, Te) composition for solar hydrogen production / E. V. Sukhanova, N. Sagatov, A. S. Oreshonkov [и др.] // Int. J. Hydrog. Energy. - 2023. - Vol. 48, Is. 38. - P. 14226-14237, DOI 10.1016/j.ijhydene.2022.12.286. - Cited References: 97. - The authors acknowledge financial support from Russian Science Foundation (№ 21-73-20183). The authors are grateful to the Joint Supercomputer Center of the Russian Academy of Sciences and to the Information Technology Centre of Novosibirsk State University for providing access to the cluster computational resources . - ISSN 0360-3199. - ISSN 1879-3487
Кл.слова (ненормированные):
Photocatalytic water splitting -- Novel materials -- Transition metal dichalcogenides -- H2 generation
Аннотация: The successful fabrication of H-phase Janus transition metal dichalcogenides (TMDs) has received considerable interest due to its great potential in photocatalytic applications. Here, new A′-XMoY (X/Y = O, S, Se, Te) Janus-type structures belonging to the family of TMDs were theoretically investigated for the first time in terms of photocatalytic water splitting via DFT calculations. For all compounds, the Raman spectra were calculated. The SMoO, SeMoO, SMoSe, SMoTe and SeMoTe compounds are dynamically stable and are semiconductors. Among all considered structures SMoTe is the most promising candidate for solar hydrogen production because valence and conduction bands perfectly engulf the redox potentials of water at both neutral and acidic media, opposite to SMoSe, SMoO, SeMoO suitable only in the acidic media, and SeMoTe – in the neutral media. Moreover, A′-SMoTe demonstrates the outstanding values of the solar-to-hydrogen (STH) conversion efficiencies of 54.0 and 67.1 for neutral and acidic media.

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Держатели документа:
Emanuel Institute of Biochemical Physics of Russian Academy of Sciences, 119334 Moscow, Russia
Sobolev Institute of Geology and Mineralogy, Siberian Branch of Russian Academy of Sciences, prosp. acad. Koptyuga 3, 630090 Novosibirsk, Russia
Laboratory of Molecular Spectroscopy, Kirensky Institute of Physics, Federal Research Center KSC SB RAS, 660036 Krasnoyarsk, Russia
School of Engineering and Construction, Siberian Federal University, 660041 Krasnoyarsk, Russia
Novosibirsk State University, Pirogova 2, 630090 Novosibirsk, Russia

Доп.точки доступа:
Sukhanova, E.V.; Sagatov, N.; Oreshonkov, A. S.; Орешонков, Александр Сергеевич; Gavryushkin, P.N.; Popov, Z.I.
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High-pressure transformation of dithiazolylidene-dithiazolium polyiodide with N-H…N hydrogen bond: A Raman spectroscopy study / I. D. Yushina, A. S. Krylov, O. I. Bol'shakov [et al.] // Spectrochim. Acta A. - 2022. - Vol. 268. - Ст. 120635, DOI 10.1016/j.saa.2021.120635. - Cited References: 24. - This work was supported by the Ministry of Science and High Education of Russian Federation, project FENU-2020-0019 . - ISSN 1386-1425
Кл.слова (ненормированные):
Polyiodides -- High pressure -- Hydrogen bond -- 1,2,3-dithiazoles
Аннотация: The insight into the behavior of polyiodides under non-ambient conditions can enrich the practical applications due to obtaining materials with adjustable and tunable conducting properties. In this work Raman spectroscopy study in the range 0 – 6.5 GPa has been performed for dithiazolylidene-dithiazolium zigzag polyiodide with N-H…N hydrogen bond. Variations of band positions in the low-wavenumber region of Raman spectra have been attributed to the changes in the anionic part of the unit cell. The association of different interacting polyiodide subunits at pressure above 1.5 GPa leads to the emergence of the bands at 98 and 115 cm−1 due to consistent vibrations in the I82- zigzag. The emergence of the band at 159 cm−1 above 0.28 GPa can be assigned to N-H…N hydrogen bond vibration. The obtained results depict undergoing structure transformations: the stronger are cation…cation and anion…anion interactions the more likely is the observation of conducting properties due to the formation of polyiodide zigzag and strongly-bound hydrogen-bonded fragment.

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Держатели документа:
South Ural State University, Chemical Faculty. 454080, Lenin avenue, 76, Chelyabinsk, Russian Federation
Kirensky Institute of Physics, Federal Research Center KSC SB RAS, Krasnoyarsk, 660036, Russian Federation
N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow, 119991, Russian Federation

Доп.точки доступа:
Yushina, I. D.; Krylov, A. S.; Крылов, Александр Сергеевич; Bol'shakov, O. I.; Rakitin, O. A.; Bartashevich, E. V.
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Nekrasov, I.
Hydrides under high pressure / I. Nekrasov, S. Ovchinnikov // J. Supercond. Nov. Magn. - 2022. - Vol. 35, Is. 4 : Road to Room Temperature Superconductivity. - P. 959-963, DOI 10.1007/s10948-021-06087-3. - Cited References: 44. - This work was partially supported by RFBR grant No. 20-02-00011 . - ISSN 1557-1939
Кл.слова (ненормированные):
Room-temperature superconductors -- High temperature superconductors -- Superconducting hydrades under high pressure -- BCS theory -- Metallic hydrogen -- Superconducting hydrogen
Аннотация: The experimental discovery of the highest, up to 0 degree Celsius, superconducting transition temperatures Tc in the class of so-called hydrides under high pressure is undoubtedly the striking event in modern physics. In this paper, we give a short overview of the some history of the room-temperature conventional superconductivity. A theoretical description of such high Tc, as was shown and even predicted in a number of ab initio works, can be unambiguously given in the framework of the electron–phonon mechanism of Cooper pairing. Thus, the basic equation to calculate Tc will be the one proposed in 1957 by Bardeen, Cooper, and Schriefer. It is known that in this case the value of Tc is directly determined by a number of effective parameters: the Debye frequency, the density of electronic states at the Fermi level, and the electron–phonon interaction constant. Within the framework of the modern development of the density functional theory, all these quantities can be obtained using standard packages for band structure calculations.

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Держатели документа:
Institute of Electrophysics, Russian Academy of Sciences, Ural Branch, Amundsena 106, Ekaterinburg, 620016, Russian Federation
Kirensky Institute of Physics, Federal Research Center KSC SB RAS, Akademgorodok, Krasnoyarsk, 660036, Russian Federation
Siberian Federal University, 79 Svobodny Pr., Krasnoyarsk, 660041, Russian Federation

Доп.точки доступа:
Ovchinnikov, S. G.; Овчинников, Сергей Геннадьевич
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Broadband Tamm plasmons in chirped photonic crystals for light-induced water splitting / M. V. Pyatnov, R. G. Bikbaev, I. V. Timofeev [et al.] // Nanomaterials. - 2022. - Vol. 12, Is. 6. - Ст. 928, DOI 10.3390/nano12060928. - Cited References: 41 . - ISSN 2079-4991
Кл.слова (ненормированные):
water splitting -- plasmon catalysis -- solar-to-hydrogen efficiency -- photocurrent
Аннотация: An electrode of a light-induced cell for water splitting based on a broadband Tamm plasmon polariton localized at the interface between a thin TiN layer and a chirped photonic crystal has been developed. To facilitate the injection of hot electrons from the metal layer by decreasing the Schottky barrier, a thin n-Si film is embedded between the metal layer and multilayer mirror. The chipping of a multilayer mirror provides a large band gap and, as a result, leads to an increase in the integral absorption from 52 to 60 percent in the wavelength range from 700 to 1400 nm. It was shown that the photoresponsivity of the device is 32.1 mA/W, and solar to hydrogen efficiency is 3.95%.

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Держатели документа:
Kirensky Institute of Physics, Krasnoyarsk Scientific Center, Siberian Branch, Russian Academy of Sciences, Krasnoyarsk, 660036, Russian Federation
Siberian Federal University, Krasnoyarsk, 660041, Russian Federation
Institute of Computer Modelling, Krasnoyarsk Scientific Center, Siberian Branch, Russian Academy of Sciences, Krasnoyarsk, 660036, Russian Federation

Доп.точки доступа:
Pyatnov, M. V.; Пятнов, Максим Владимирович; Bikbaev, R. G.; Бикбаев, Рашид Гельмединович; Timofeev, I. V.; Тимофеев, Иван Владимирович; Ryzhkov, I. I.; Vetrov, S. Ya.; Ветров, Степан Яковлевич; Shabanov, V. F.; Шабанов, Василий Филиппович
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Dynamic processes of the water sublattice in FeTiF6·xH2O·yD2O crystal / Yu. V. Gerasimova, A. S. Krylov, A. N. Vtyurin [et al.] // J. Raman Spectrosc. - 2022. - Vol. 53, Is. 10 : Special Issue: Vibrational Spectroscopy of Water. - P. 1704-1709, DOI 10.1002/jrs.6430. - Cited References: 31. - The reported study was funded by the Russian Foundation for Basic Research, Government of Krasnoyarsk Territory and Krasnoyarsk Regional Foundation of Science according to the research project “Spectral and magnetic properties of single crystals of transition metal fluoride hexahydrates” No. 20-42-240014 . - ISSN 0377-0486
Кл.слова (ненормированные):
deuterium ordering -- dynamics -- hydrated iron fluoridotitanate -- hydrogen bonds -- phase transition -- spectra -- water sublattice
Аннотация: Phase transition in FeTiF6·xH2O·yD2O crystals has been studied by Raman spectroscopy. The 611 cm-1 line corresponding to mode A1g of [TiF6]2- system does not exhibit anomalous behavior associated with the phase transition. The temperature studies showed that below the phase transition temperature, the equivalence of D2O molecules in FeTiF6·xH2O·yD2O octahedron is broken. The phase transition mechanism in the compound under study is associated with Fe(xH2O·yD2O) complex.

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Держатели документа:
Kirensky Institute of Physics, Siberian Branch of RAS, Krasnoyarsk, Russian Federation
Institute of Engineering Physics and Radio Electronics, Siberian Federal University, Krasnoyarsk, Russian Federation
Institute of Chemistry, Far Eastern Branch of RAS, Vladivostok, Russian Federation

Доп.точки доступа:
Gerasimova, Yu. V.; Герасимова, Юлия Валентиновна; Krylov, A. S.; Крылов, Александр Сергеевич; Vtyurin, A. N.; Втюрин, Александр Николаевич; Laptash, N. M.; Pogoreltsev, E. I.; Погорельцев, Евгений Ильич; Dubrovskiy, A. A.; Дубровский, Андрей Александрович; Gerasimov, M. A.; Герасимов, М. А.
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    Пятнов, Максим Владимирович.
    Фотоэлектрохимическое расщепление воды наноструктурированным электродом и зеленая водородная энергетика / М. В. Пятнов, И. В. Тимофеев // Фотоника. - 2022. - Т. 16, Вып. 2. - С. 116-125 ; Photonics Rus., DOI 10.22184/1993-7296.FRos.2022.16.2.116.125. - Библиогр.: 28. - Исследование выполнено за счет гранта Российского научного фонда и Красноярского краевого фонда поддержки научной и научно-технической деятельности № 22-22-20078, https://rscf.ru/project/22-22-20078 . - ISSN 1993-7296. - ISSN 2686-844X
   Перевод заглавия: Photoelectrochemical water splitting by a nanostructured electrode and green hydrogen energy
Кл.слова (ненормированные):
плазмонный катализ -- расщепление воды -- фототок -- эффективность преобразования света в водород -- plasmonic catalysis -- water splitting -- photo-induced current -- light-to-hydrogen conversion efficiency
Аннотация: В статье описан перспективный способ получения водорода – фотоэлектрохимическое расщепление воды. Этот подход сочетает непосредственное использование солнечной энергии и низкую стоимость производства фотоэлектрохимических ячеек из широко распространенных на Земле полупроводниковых материалов. Последние достижения в конструировании таких ячеек включают наноструктурирование полупроводниковых электродов плазмонными материалами.
This article describes a promising hydrogen formation method, namely the photoelectrochemical water splitting. This approach combines the direct use of solar energy and low production cost of photoelectrochemical cells using the widely used semiconductor materials. The latest advances in such cell design include nanostructuring of the semiconductor electrodes with plasmonic materials.

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Держатели документа:
Институт физики им. Л. В. Киренского СО РАН -обособленное подразделение ФИЦ КНЦ СО РАН
Сибирский федеральный университет

Доп.точки доступа:
Тимофеев, Иван Владимирович; Timofeev, I. V.; Pyatnov, M. V.

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10.

    Obtaining particles with the structure Mg@C and (Mg@C)@Pd, their properties and stability in the hydrogenation/dehydrogenation processes / G. N. Churilov, N. S. Nikolaev, V. I. Elesina [et al.] // Int. J. Hydrogen Energy. - 2022. - Vol. 47. Is. 11. - P. 7299-7309, DOI 10.1016/j.ijhydene.2021.03.042. - Cited References: 46 . - ISSN 0360-3199
   Перевод заглавия: Получение частиц со структурой Mg@C и (Mg@C)@Pd, их свойства и стабильность в процессах гидрирования /дегидрирования
Кл.слова (ненормированные):
Core-shell particles -- Mg, С, Рd nanoparticles -- Sorption capacity of hydrogen -- Hydrogen-storage materials -- Magnesium hydride
Аннотация: In this work, we studied the change in the properties of powders with a core (magnesium) – shell structure (carbon and carbon/palladium) in the process of hydrogenation/dehydrogenation with hydrogen (99.995 wt%). Magnesium powders were obtained by plasma chemical synthesis in an atmosphere of argon containing a small amount of hydrogen (2–3 at.%) and nitrogen (8–9 at.%), when performing a low-frequency arc discharge between a tungsten electrode and a magnesium melt. The shell (carbon and carbon/palladium) was deposited in a plasma generator with vortex and magnetic stabilization. For all samples, a decrease in the sorption capacity of hydrogen was observed as a result of successive cycles of sorption and desorption reactions. It was found that the reason for this fall is associated with the formation of the MgO and Mg(OH)2 phase, which prevents the diffusion of hydrogen. The carbon shell provides a more complete hydrogenation of the magnesium particles, and an additional palladium shell increases the resistance to cyclic hydrogenation/dehydrogenation and reduces the temperature of these processes. According to the data obtained, powders with particles (Mg@C)@Pd can absorb the largest amount of hydrogen (6.9 wt%) for the duration of 5 cycles, after which the protective shell of the particles begins to collapse and a loss of sorption capacity is observed.

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Держатели документа:
Institute of Engineering Physics and Radio Electronics, Siberian Federal University, Svobodny, 79, Krasnoyarsk, 660041, Russian Federation
Kirensky Institute of Physics, Federal Research Center KSC SB RAS, Akademgorodok 50/38, Krasnoyarsk, 660036, Russian Federation
Institute of Chemistry and Chemical Technology, Federal Research Center KSC SB RAS, Akademgorodok 50/24, Krasnoyarsk, 660036, Russian Federation

Доп.точки доступа:
Churilov, G. N.; Чурилов, Григорий Николаевич; Nikolaev, N. S.; Николаев, Никита Сергеевич; Elesina, V. I.; Елесина, Виктория Игоревна; Glushenko, G. A.; Глущенко, Гарий Анатольевич; Isakova, V. G.; Исакова, Виктория Гавриловна; Tomashevich, Y. V.
}
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11.

    Induced magnetic anisotropy of Co-P thin films obtained by electroless deposition / A. V. Chzhan, S. A. Podorozhnyak, S. M. Zharkov [et al.] // J. Magn. Magn. Mater. - 2021. - Vol. 537. - Ст. 168129, DOI 10.1016/j.jmmm.2021.168129. - Cited References: 28. - The work is partially supported by the RFBR Foundation (10-02-00161-a project). The study has been carried out within the framework of the state task of the Ministry of science and higher education of the Russian Federation (topic No. FSRZ-2020-0011) . - ISSN 0304-8853
   Перевод заглавия: Индуцированная магнитная анизотропия тонких пленок Co-P, полученных химическим осаждением
Кл.слова (ненормированные):
Cobalt -- Cobalt compounds -- Coercive force -- Drops -- Electroless plating -- Magnetic anisotropy -- Magnetic fields -- Cover glass -- Deposition of films -- Diffraction peaks -- Electroless -- Hydrogen indices -- Induced magnetic anisotropy -- Magnetic anisotropy constant -- pH range -- Thin-films
Аннотация: Co1−x-Px films (x = 0.02–0.05) deposited on cover glass by electroless plating from aqueous solutions in a continuous magnetic field with the strength of 2.5 kOe are presented. It has been found that in the pH range from 7.2 to 9.3, two special areas can be distinguished, they are characterized by the deposition of films with qualitatively different parameters in them. So, the change of the pH of working solutions from 7.2 to 8.7 causes the increase in the value of the induced magnetic anisotropy constant KU from 2.5 × 105 erg/cm3 to 6 × 105 erg/cm3. If the value of the hydrogen index is still increasing, an uneven drop to 5 × 104 erg/cm3 is observed. In the same way, the coercivity HC changes; at first it grows from 700 Oe to 1.5 kOe, and then it drops to Oe units. The concentration of phosphorus in the range of 7.2 to 8.7 increases linearly from 2 to 3 wt%, and in the range of 8.7 to 9.3, it increases from 3 to 5 wt%. The x-ray diffraction data show that the samples obtained at pH<8.7 are characterized by the presence of the hcp phase of Co (α-Co). The observed reflections of films obtained at pH > 8.7 indicate the fcc-Co (β-Co) with the diffraction peak blurring: the greater the pH value of the samples obtained, the more the diffraction peak blurring. It is shown that the induced magnetic anisotropy in high-coercivity films relates to the modification of the Co lattice. The lattice passes from a distorted fcc to an hcp structure during the growth of crystallites in a magnetic field. The induced magnetic anisotropy appears in films that were obtained in the high pH field due to the ordering of magnetic ions pairs.

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Держатели документа:
Siberian Federal University, Krasnoyarsk, Russian Federation
Krasnoyarsk State Agrarian University, Krasnoyarsk, Russian Federation
Kirensky Institute of Physics, Federal Research Center KSC SB RAS, Krasnoyarsk, Russian Federation
Nikolaev Institute of Inorganic Chemistry SB RAS, ave. Lavrentyev 3, Novosibirsk, Russian Federation

Доп.точки доступа:
Chzhan, A. V.; Podorozhnyak, S. A.; Zharkov, S. M.; Жарков, Сергей Михайлович; Gromilov, S. A.; Patrin, G. S.; Патрин, Геннадий Семёнович
}
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12.

    Role of metal-chloride anions in photoluminescence regulations for hybrid metal halides / B. Su, G. Song, M. S. Molokeev [et al.] // J. Phys. Chem. Lett. - 2021. - Vol. 12, Is. 7. - P. 1918-1925, DOI 10.1021/acs.jpclett.1c00182. - Cited References: 40. - This work is supported by the National Natural Science Foundation of China (51961145101 and 51972118), the Fundamental Research Funds for the Central Universities (D2190980), the Guangzhou Science & Technology Project (202007020005), and the Local Innovative and Research Teams Project of Guangdong Pearl River Talents Program (2017BT01X137). This work is also funded by RFBR according to the research project No. 19-52-80003 . - ISSN 1948-7185
   Перевод заглавия: Роль металл-хлорид-анионов в регуляции фотолюминесценции гибридных галогенидов металлов
Кл.слова (ненормированные):
Intra-molecular hydrogen bonds -- Intramolecular interactions -- Luminescence mechanisms -- Organic-inorganic hybrid -- Photoluminescence properties -- Photoluminescence quantum yields -- Photophysical properties -- Structural diversity -- Metal halides
Аннотация: Organic–inorganic hybrid metal halides with emissive organic cations are of great interest due to their structural diversity and interesting photophysical properties. Here, we assemble emissive organic cations (EnrofloH22+) with different metal–chloride anions (Pb2Cl62– to Bi2Cl104– to SnCl62–) to form the new single crystal phases, and thus the photoluminescence properties of the metal halides, including Stokes shift, full width at half-maximum (FWHM), and photoluminescence quantum yield (PLQY) have been studied accordingly. (EnrofloH2)SnCl6·H2O, as an example, possesses narrow FWHM and high PLQY, which are caused by the strong π–π stacking and inter- and intramolecular hydrogen bonds interactions. Compared with EnrofloH22+ cation in solution, the interactions generate a restraining effect and increase the rigid degree of EnrofloH22+ cation in the bulk single crystals. Our work clarifies the photophysical properties of the EnrofloH22+ organic cations by constructing the inter- and intramolecular interactions and boosts the further study of organic–inorganic hybrid metal halides materials with different luminescence mechanisms.

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Держатели документа:
The State Key Laboratory of Luminescent Materials and Devices, Guangdong Provincial Key Laboratory of Fiber Laser Materials and Applied Techniques, School of Materials Science and Technology, South China University of Technology, Guangzhou, 510640, China
Technical Institute of Physics and Chemistry, University of Chinese Academy of Sciences, Beijing, 100190, China
Center of Materials Science and Optoelectronics Engineering, University of the Chinese Academy of Sciences, Beijing, 100049, China
Laboratory of Crystal Physics, Kirensky Institute of Physics, Federal Research Center KSC SB RAS, Krasnoyarsk, 660036, Russian Federation
Siberian Federal University, Krasnoyarsk, 660041, Russian Federation
Research and Development Department, Kemerovo State University, Kemerovo, 650000, Russian Federation

Доп.точки доступа:
Su, B.; Song, G.; Molokeev, M. S.; Молокеев, Максим Сергеевич; Golovnev, N. N.; Lesnikov, M. K.; Lin, Z.; Xia, Z.
}
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13.

Hydrogen bond effects in multimode nuclear dynamics of acetic acid observed via resonant x-ray scattering / V. Savchenko, V. Ekholm, I. E. Brumboiu [et al.] // J. Chem. Phys. - 2021. - Vol. 154, Is. 21. - Ст. 214304, DOI 10.1063/5.0049966. - Cited References: 64. - This work was supported by the Swedish Research Council (Grant Nos. 2019-03470, 2018-4343, and 2017-06419) and the Russian Science Foundation (Project No. 16-12-10109). M.O. acknowledges financial support from the Carl Tryggers Foundation (Grant CTS18:285) and the European Union’s Horizon 2020 research and innovation programme under the Marie Skłodowska-Curie Grant Agreement No. 860553. F.G. acknowledges the support from the Helmholtz Virtual Institute VI419 “Dynamic Pathways in Multidimensional Landscapes.” The research work of V.S. was partially funded by a Swedish Institute scholarship. The synchrotron experiments were performed at the ADRESS beamline of the Swiss Light Source at the Paul Scherrr Institut (PSI). The work at PSI was supported by the Swiss National Science Foundation through the NCCR MARVEL and the Sinergia project “Mott Physics Beyond the Heisenberg (MPBH) model” (SNSF Research Grant Nos. CRSII2:141962 and CRSII2:1607651). The research leading to these results received funding from the European Community’s Seventh Framework Programme (No. FP7/2007–2013) under Grant Agreement No. 290605 (COFUND: PSIFELLOW). The calculations were enabled by resources provided by the Swedish National Infrastructure for Computing (SNIC) partially funded by the Swedish Research Council through Grant Agreement No. 2018-05973 . - ISSN 0021-9606
Кл.слова (ненормированные):
Acetic acid -- Degrees of freedom (mechanics) -- Dimers -- Hydrogen bonds -- Liquids -- pH -- Comprehensive analysis -- Hydrogen-bond effect -- Hydrogen-bond formation -- Resonant inelastic x-ray scattering -- Resonant X-ray scattering -- Theoretical simulation -- Vibrational degrees of freedom -- Vibrational dynamics -- X ray scattering
Аннотация: A theoretical and experimental study of the gas phase and liquid acetic acid based on resonant inelastic x-ray scattering (RIXS) spectroscopy is presented. We combine and compare different levels of theory for an isolated molecule for a comprehensive analysis, including electronic and vibrational degrees of freedom. The excitation energy scan over the oxygen K-edge absorption reveals nuclear dynamic effects in the core-excited and final electronic states. The theoretical simulations for the monomer and two different forms of the dimer are compared against high-resolution experimental data for pure liquid acetic acid. We show that the theoretical model based on a dimer describes the hydrogen bond formation in the liquid phase well and that this bond formation sufficiently alters the RIXS spectra, allowing us to trace these effects directly from the experiment. Multimode vibrational dynamics is accounted for in our simulations by using a hybrid time-dependent stationary approach for the quantum nuclear wave packet simulations, showing the important role it plays in RIXS.

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Держатели документа:
Department of Theoretical Chemistry and Biology, Kth Royal Institute of Technology, Stockholm, SE-106 91, Sweden
International Research Center of Spectroscopy and Quantum Chemistry-IRC Sqc, Siberian Federal University, Krasnoyarsk, 660041, Russian Federation
Kirensky Institute of Physics, Federal Research Center Ksc Sb Ras, Krasnoyarsk, 660036, Russian Federation
Department of Physics and Astronomy, Uppsala University, P.O. Box 516, Uppsala, SE-751 20, Sweden
Max Iv Laboratory, Lund University, P.O. Box 118, Lund, SE-221 00, Sweden
Department of Chemistry, Pohang University of Science and Technology (POSTECH), Pohang, 37673, South Korea
Institute for Methods and Instrumentation in Synchrotron Radiation Research PS-ISRR, Helmholtz-Zentrum Berlin fur Materialien und Energie, Albert-Einstein-Strasse 15, Berlin, 12489, Germany
Institut fur Physik und Astronomie, Universitat Potsdam, Karl-Liebknecht-Strasse 24-25, Potsdam, 14476, Germany
Department of Medicinal Chemistry, Uppsala University, P.O. Box 574, Uppsala, 75123, Sweden
Swiss Light Source, Photon Science Division, Paul Scherrer Institut, Villigen PSI, CH-5232, Switzerland
Department of Physics, Stockholm University, AlbaNova University Center, Stockholm, 10691, Sweden

Доп.точки доступа:
Savchenko, V.; Савченко, Виктория; Ekholm, V.; Brumboiu, I. E.; Norman, P.; Pietzsch, A.; Fohlisch, A.; Rubensson, J. -E.; Grasjo, J.; Bjorneholm, O.; Sathe, C.; Dong, M.; Schmitt, T.; McNally, D.; Lu, X.; Krasnov, P. O.; Краснов, Павел Олегович; Polyutov, S. P.; Полютов, Сергей Петрович; Gel'mukhanov, F.; Гельмуханов, Фарис Хафизович; Odelius, M.; Kimberg, V.; Кимберг, Виктор Валерьевич
}
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14.

    Heterostructures based on Pd–Au nanoparticles and cobalt phthalocyanine for hydrogen chemiresistive sensors / N. S. Nikolaeva, D. D. Klyamer, S. M. Zharkov [et al.] // Int. J. Hydrogen Energy. - 2021. - Vol. 46. Is. 37. - P. 19682-19692, DOI 10.1016/j.ijhydene.2021.03.082. - Cited References: 74. - The work on the synthesis of Au MOCVD precursor and deposition of gold nanoparticles on various surfaces were funded by Russian Science Foundation (RSF) (research project № 20-15-00222 ). The TEM and electron diffraction investigations were conducted in the SFU Joint Scientific Center supported by the State assignment ( #FSRZ-2020-0011 ) of the Ministry of Science and Higher Education of the Russian Federation . - ISSN 0360-3199
   Перевод заглавия: Гетероструктуры, основанные на наночастицах Pd-Au и фтолоцианине кобальта, для хемирезисторных сенсоров водорода
Кл.слова (ненормированные):
Palladium nanoparticles -- Gold nanoparticles -- Bimetallic nanoparticles -- Metal phthalocyanine -- Chemiresistive sensors -- Hydrogen
Аннотация: In this work, the effect of Pd, Au and PdAu nanoparticles on sensor response of cobalt phthalocyanine films to hydrogen was studied. For this purpose, novel heterostructures based on cobalt phthalocyanine and PdAu nanoalloys were obtained by a combination of vacuum thermal evaporation and pulsed metalorganic chemical vapor deposition (MOCVD) and investigated as active layers for hydrogen detection. The structural features and phase composition of the prepared heterostructures were studied by the techniques of X-ray diffraction, transmission electron microscopy and electron diffraction. The concentration of metal nanoparticles in the samples was determined by inductively coupled plasma atomic emission spectroscopy (ICP-AES). The chemiresistive sensor response of CoPc/M (M = Pd, Au, Pd0.2Au0.8 and Pd0.8Au0.2) to hydrogen (100–400 ppm, room temperature) was compared with that of bare CoPc films. It was shown that the sensor response of the investigated heterostructures to hydrogen (300 ppm) increased in the order CoPc (0.2%) < CoPc/Pd0.2Au0.8 (1.9%) ~ CoPc/Au (2.2%) < CoPc/Pd (2.7%) < CoPc/Pd0.8Au0.2 (5.6%).

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Держатели документа:
Nikolaev Institutes of Inorganic Chemistry SB RAS, Lavrentiev Pr. 3, Novosibirsk, 630090, Russian Federation
Kirensky Institute of Physics, Federal Research Center KSC SB RAS, Akademgorodok 50/38, Krasnoyarsk, 660036, Russian Federation
Siberian Federal University, 79 Svobodny pr., Krasnoyarsk, 660041, Russian Federation

Доп.точки доступа:
Nikolaeva, N. S.; Klyamer, D. D.; Zharkov, S. M.; Жарков, Сергей Михайлович; Tsygankova, A. R.; Sukhikh, A. S.; Morozova, N. B.; Basova, T. V.
}
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15.

    New titania-based photocatalysts for hydrogen production from aqueous-alcoholic solutions of methylene blue / D. V. Markovskaya, A. V. Zhurenok, A. Y. Kurenkova [et al.] // RSC Adv. - 2020. - Vol. 10, Is. 56. - P. 34137-34148, DOI 10.1039/d0ra07630a. - Cited References: 57. - The XPS and XRD experiments were performed using facilities of the shared research center "National center for investigation of catalysts" at Boreskov Institute of Catalysis. The authors are grateful to Dr S. Cherepanova for the XRD study and Dr T. Larina and Dr D. Selishchev for the UV-vis measurements. The TEM investigations were conducted in the SFU Joint Scientific Center supported by the State assignment (#FSRZ-2020-0011) of the Ministry of Science and Higher Education of the Russian Federation . - ISSN 2046-2069
   Перевод заглавия: Новые катализаторы, основанные на диоксиде титана, для производства водорода из водно-спиртовых растворов метиленовой сини

РУБ Chemistry, Multidisciplinary
Рубрики:
Ray absorption-edge
   In-situ
   Ag nanoparticles
   Chemical-states
   XPS analysis
Аннотация: A series of CuOx–TiO2 photocatalysts were prepared using fresh and thermally activated Evonik Aeroxide P25 titanium dioxide. The photocatalysts were characterized by X-ray diffraction, transmission electron microscopy, X-ray photoelectron spectroscopy, XANES, diffuse reflectance spectroscopy, and N2 adsorption technique. Photocatalytic activity of the samples was tested in hydrogen production from aqueous-alcoholic solutions of methylene blue under UV radiation (λ = 386 nm). It was found for the first time the synergistic effect of hydrogen production from two substrates—dye and ethanol. The maximum hydrogen production rate in the system water–ethanol–methylene blue was 1 μmol min−1, which is 25 times higher than a value measured in a 10% solution of ethanol in water. The thermal activation of titania also leads to a change in the rate of hydrogen production. The highest catalytic activity was observed for a CuOx–TiO2 photocatalyst based on titania thermally-activated at 600 °C in air. A mechanism of the photocatalytic reaction is discussed.

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Держатели документа:
Boreskov Inst Catalysis, Fed Res Ctr, Lavrentiev Ave 5, Novosibirsk 630090, Russia.
Fed Res Ctr KSC SB RAS, Kirensky Inst Phys, Akademgorodok 50-38, Krasnoyarsk 660036, Russia.
Siberian Fed Univ, 79 Svobodny Pr, Krasnoyarsk 660041, Russia.

Доп.точки доступа:
Markovskaya, Dina, V; Zhurenok, Angelina, V; Kurenkova, Anna Yu; Kremneva, Anna M.; Saraev, Andrey A.; Zharkov, S. M.; Жарков, Сергей Михайлович; Kozlova, Ekaterina A.; Kaichev, Vasily V.
}
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16.

Anisotropy of piezocaloric effect at ferroelectric phase transitions in ammonium hydrogen sulphate / E. A. Mikhaleva, M. V. Gorev, M. S. Molokeev [et al.] // J. Alloys Compd. - 2020. - Vol. 839. - Ст. 155085, DOI 10.1016/j.jallcom.2020.155085. - Cited References: 31. - The reported study was supported by the Russian Science Foundation (project no. 19-72-00023 ). X-ray and dilatometric data were obtained using the equipment of Krasnoyarsk Regional Center of Research Equipment of Federal Research Center "Krasnoyarsk Science Center SB RAS" . - ISSN 0925-8388
Кл.слова (ненормированные):
Piezocaloric effect -- Phase transition -- Ferroelectrics -- Thermal expansion -- High-pressure -- Entropy
Аннотация: The role of anisotropy of the thermal expansion in formation of piezocaloric effect (PCE) near ferroelectric phase transitions in NH4HSO4 was studied. Strong difference in linear baric coefficients and as a result in intensive and extensive PCE associated with the different crystallographic axes was found. PCE giving the main contribution to the barocaloric effect were determined at both phase transitions. Rather strong effect of the lattice dilatation on the tuning of PCE was observed. Comparative analysis of PCE at the phase transitions in different materials showed that NH4HSO4 can be considered as a promising solid-state refrigerant. A hypothetical cooling cycle based on alternate using uniaxial pressure along two axes was considered.

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Держатели документа:
Kirensky Institute of Physics, Federal Research Center KSC SB RAS, Krasnoyarsk, 660036, Russian Federation
Institute of Engineering Physics and Radioelectronics, Siberian Federal University, Krasnoyarsk, 660074, Russian Federation
Department of Physics, Far Eastern State Transport University, Khabarovsk, 680021, Russian Federation
Astafijev Krasnoyarsk State Pedagogical University, Krasnoyarsk, 660049, Russian Federation

Доп.точки доступа:
Mikhaleva, E. A.; Михалева, Екатерина Андреевна; Gorev, M. V.; Горев, Михаил Васильевич; Molokeev, M. S.; Молокеев, Максим Сергеевич; Kartashev, A. V.; Карташев, Андрей Васильевич; Flerov, I. N.; Флёров, Игорь Николаевич
}
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17.

    Golovnev, N. N.
    Three isomers in a (hydrogen L-Cysteinato)-thallium(I): Crystal structure, spectroscopic and thermal properties / N. N. Golovnev, M. S. Molokeev, M. K. Lesnikov // Polyhedron. - 2019. - Vol. 173. - Ст. 114141, DOI 10.1016/j.poly.2019.114141. - Cited References: 37. - The study was carried out within the public task of the Ministry of Education and Science of the Russian Federation to the Siberian Federal University (4.7666.2017/BP) in 2017–2019. X-ray data from single crystals and powder pattern were obtained with use the analytical equipment of Krasnoyarsk Center of collective use of SB RAS. . - ISSN 0277-5387
   Перевод заглавия: Три изомера в (H L-цистеин)-таллии(I): кристаллическая структура, спектроскопические и термические свойства
Кл.слова (ненормированные):
Cysteine -- Thallium -- Complex -- Isomers -- Structre
Аннотация: The isolation of thallium(I) complexes [Tl2(HCys)2]n (1) and [Tl4(HCys)4]n (2) {H2Cys = l-Cysteine} from aqueous solution by means of crystallization is reported herein. Polar crystals of 1 and 2 were crystallized in P21 and P212121 space groups respectively. Elemental analysis, XRD, IR, UV–Vis, TG-DSC and a single crystal X-ray diffraction were applied for characterizing the compounds. Linkage isomers 1 and 2 have 1D and 2D coordination polymeric structures respectively. The lone pair electrons of thallium(I) in 1–2 are stereo-chemically active. In 1, each of two independent Tl+ ions is coordinated by three HCys− ions forming TlS3O irregular polyhedron that is linked to each other by vertexes in an infinite chain. In 2, four independent Tl+ ions are coordinated by HCys− ions through S and O atoms, forming Tl1S3O2, Tl2S4, Tl3S3, Tl4S3 irregular polyhedrons. The crystallographic independent HCys− ions are linked to the metal ion differently, two are μ3-S,S,S-, one is μ4-O,S,S,S-, and one is μ4-O,O',S,S,S-coordinated ligands. The amine group of compounds 1 and 2 is in the form of an ammonium ion (–NH3+). The structures of 1–2 are stabilized by NH⋯O hydrogen bonds, thallophilic Tl⋯Tl and anagostic Tl⋯HC interactions. The spectroscopic and thermal properties of compounds were analyzed.

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Держатели документа:
Department of Chemistry, Siberian Federal University, 79 Svobodny Ave., Krasnoyarsk, 660041, Russian Federation
Laboratory of Crystal Physics, Kirensky Institute of Physics, Federal Research Center KSC SB RAS, Bld. 38 Akademgorodok 50, Krasnoyarsk, 660036, Russian Federation
Department of Engineering Physics and Radioelectronic, Siberian Federal University, 79 Svobodny Ave., Krasnoyarsk, 660041, Russian Federation
Department of Physics, Far Eastern State Transport University, 47 Seryshev Str., Khabarovsk, 680021, Russian Federation

Доп.точки доступа:
Molokeev, M. S.; Молокеев, Максим Сергеевич; Lesnikov, M. K.
}
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18.

Anisotropy of piezocaloric effect at ferroelectric phase transitions in ammonium hydrogen sulphate / E. V. Bogdanov, I. N. Flerov // E-MRS fall meeting : conference programme. - 2019. - Ст. E.P.4. - This work was supported by the Russian Science Foundation (RSF) grant (No. 19-72-00023)

Материалы конференции
Держатели документа:
Kirensky Institute of Physics, Federal Research Center KSC SB RAS, 660036 Krasnoyarsk, Russia
Siberian Federal University, 660074 Krasnoyarsk, Russia
Far Eastern State Transport University, Khabarovsk, Russia 680021
Astafijev Krasnoyarsk State Pedagogical University, 660049 Krasnoyarsk, Russia

Доп.точки доступа:
Mikhaleva, E. A.; Михалева, Екатерина Андреевна; Gorev, M. V.; Горев, Михаил Васильевич; Molokeev, M. S.; Молокеев, Максим Сергеевич; Kartashev, A. V.; Карташев, Андрей Васильевич; Flerov, I. N.; Флёров, Игорь Николаевич; Fall Meeting, European Materials Research Society(2019 ; Sept. ; 16-19 ; Warsaw, Poland); European Materials Research Society; Warsaw University of Technology
}
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19.

    Giant hydrogen effect on the structure and physical properties of ZnO and Co-doped ZnO films fabricated by the RF magnetron sputtering in Ar + H2 atmosphere / I. S. Edelman [et al.] // J. Magn. Magn. Mater. - 2019. - Vol. 489. - Ст. 165461, DOI 10.1016/j.jmmm.2019.165461. - Cited References: 39. - The work is supported by the Russian Academy of Sciences in the frames of Project No 0356-2017-0030 and by the Ministry of Science and Technology of Taiwan MOST 106-2112-M-110-001. . - ISSN 0304-8853. - ISSN 1873-4766
   Перевод заглавия: Колоссальное влияние водорода на структуру и физические свойства пленок ZnO и ZnO допированных кобальтом, полученных методом высокочастотного магнетронного распыления в атмосфере аргона и водорода

РУБ Materials Science, Multidisciplinary + Physics, Condensed Matter
Рубрики:
MAGNETOOPTICAL PROPERTIES
OPTICAL-PROPERTIES
FERROMAGNETISM
Кл.слова (ненормированные):
ZnO films -- Co-doped ZnO films -- Films hydrogenation -- Magnetic circular -- dichroism -- Room temperature ferromagnetism
Аннотация: ZnO and Co-doped ZnO films were synthesized by the radio frequency magnetron sputtering in mixed atmosphere of Ar + 20% O2 and Ar + 20–50% H2. The morphology, chemical composition, crystal structure, optical transmission, electrical resistance, and magnetic circular dichroism of the films were investigated. It was established that the films thickness decreased several times when Ar was partly replaced by hydrogen in the sputtering chamber. At the same time, for the Co-doped ZnO films, the increase in the relative Co content with the increasing hydrogen concentration was observed. These phenomena are explained by the formation of gaseous ZnH2 because of the hydrogen reaction with the growing films under the conditions of the high substrate temperature (450 °C) and, respectively, the decrease in the Zn component in the films. The hydrogenated Co-doped ZnO films exhibit an increase in electric conductivity and ferromagnetic behavior at room temperature. The magnetic nature of the films is explained by a combination of the intrinsic ferromagnetism (due to the formation of the Co-H-Co complex) with the inclusion of metallic Co clusters.

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Держатели документа:
Fed Res Ctr KSC SB RAS, Kirensky Inst Phys, Krasnoyarsk 660036, Russia.
Natl Sun Yat Sen Univ, Dept Phys, Kaohsiung 80424, Taiwan.
Natl Univ Kaohsiung, Dept Appl Phys, Kaohsiung 81148, Taiwan.
Siberian Fed Univ, Krasnoyarsk 660041, Russia.
ESRF, CS 40220, F-38043 Grenoble, France.

Доп.точки доступа:
Edelman, I. S.; Эдельман, Ирина Самсоновна; Chou, Hsiung; Samoshkina, Yu. E.; Самошкина, Юлия Эрнестовна; Petrov, D. A.; Петров, Дмитрий Анатольевич; Lin, Hsien C.; Chan, Wen L.; Sun, Shih-Jye; Zharkov, S. M.; Жарков, Сергей Михайлович; Bondarenko, G. V.; Бондаренко, Геннадий Васильевич; Platunov, M. S.; Платунов, Михаил Сергеевич; Rogalev, A.; Russian Academy of Sciences [0356-2017-0030]; Ministry of Science and Technology of Taiwan [MOST 106-2112-M-110-001]
}
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20.

In Situ FMR Study of the Selective H2S-Oxidation Stability of ε-Fe2O3/SiO2 Catalysts / S. S. Yakushkin [et al.] // Appl. Magn. Reson. - 2019. - Vol. 50, Is. 5. - P. 725-733, DOI 10.1007/s00723-019-1109-3. - Cited References:32. - This work was supported by the Russian Science Foundation, project no. 17-12-01111. . - ISSN 0937-9347. - ISSN 1613-7507

РУБ Physics, Atomic, Molecular & Chemical + Spectroscopy
Рубрики:
HYDROGEN-SULFIDE
   CALCINATION TEMPERATURE
   OXIDATION
   PHASE
   BED
Аннотация: The stability of a catalyst for partial H2S oxidation has been studied by the ferromagnetic resonance (FMR) technique combined with transmission electron microscopy, X-ray diffraction, Mössbauer spectroscopy, and magnetostatic investigations. The ε-Fe2O3 iron oxide nanoparticles supported on silica have been examined for their stability under the selective H2S oxidation conditions. The combination of the physicochemical methods has been used to study the state of reacted catalysts. The ε-Fe2O3 phase has been found to remain stable under the selective H2S oxidation conditions at temperatures up to 300 °C. The active phase state during the catalytic reaction has been explored using in situ FMR experiments. It has been established that the ε-Fe2O3 nanoparticles retain their structure and magnetic properties in the presence of H2S at high temperatures. During the in situ FMR experiments, the ε-Fe2O3 sulfidation process has been studied.

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Держатели документа:
Russian Acad Sci, Siberian Branch, Boreskov Inst Catalysis, Lavrentieva 5, Novosibirsk 630090, Russia.
RAS, Fed Res Ctr KSC SB, Kirensky Inst Phys, Krasnoyarsk 660036, Russia.

Доп.точки доступа:
Yakushkin, S. S.; Bukhtiyarova, G. A.; Dubrovskiy, A. A.; Дубровский, Андрей Александрович; Knyazev, Yu. V.; Князев, Юрий Владимирович; Balaev, D. A.; Балаев, Дмитрий Александрович; Martyanov, O. N.; Russian Science Foundation [17-12-01111]
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